Disease associated variation - GWASdb | Chr | Pos | SNP ID(dbSNP 142) | Ref | Alt | Ori SNP ID | P-value | Drug Name | Drug Anno | GWAS Trait | HPO ID | DO ID | AA | Type | Trait or Drug | 11 | 5535671 | rs1044392 | A | G | rs1044392 | 3.20E-18 | | | Fetal hemoglobin levels | HPOID:0001903 | DOID:12241|DOID:10923 | C | UTR-3 | GWASdb_trait | 11 | 5535671 | rs11547558 | A | AA,AG | rs1044392 | 3.20E-18 | | | Fetal hemoglobin levels | HPOID:0001903 | DOID:12241|DOID:10923 | C | UTR-3 | GWASdb_trait | 11 | 5537161 | rs2047456 | A | G | rs2047456 | 9.28E-04 | | | Common variable immunodeficiency | HPOID:0002721 | DOID:12177 | T | missense | GWASdb_trait | 11 | 5537780 | rs1809862 | C | A | rs1809862 | 3.86E-19 | | | Fetal hemoglobin levels | HPOID:0001903 | DOID:12241|DOID:10923 | G | UTR-5 | GWASdb_trait | |